MAUDE Adverse Event Report: EXACTECH, INC. EQUINOXE; RS GLENOID PLATE L POST AUG, 8 DEG, LEFT

Model Number	320-15-03
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Bacterial Infection (1735)
Date of Event	06/01/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Concomitant device(s): eq rev locking screw , 320-15-05 ,4991276; equinoxe reverse tray adapter plate tray +0, 320-10-00, 4981937; equinoxe, humeral stem primary, press fit 11mm, 300-01-11, 4977661; eq rev compress screw lck cap kit, 4.5 x 26mm , 320-20-26, 4911197; eq rev compress screw lck cap kit, 4.5 x 26mm , 320-20-26 , 4993230; eq reverse torque defining screw kit , 320-20-00 , 4981183; eq rev compress screw lck cap kit, 4.5 x 30mm , 320-20-30, 4988776; eq rev compress screw lck cap kit, 4.5 x 26mm , 320-20-26, 4911347; rs expanded glenosphere 42mm, +4mm offset , 320-02-42 , 4989979; equinoxe reverse 42mm humeral liner +0 , 320-42-00 ,4958961.
Event or Problem Description
As was reported, approximately 3.2 yrs postop the initial l tsa, this (b)(6) y/o male patient was revised.Everything was removed and a cement spacer was inserted due to infection.Affected.This product is not available for return.
Additional Manufacturer Narrative
Section h10: (h3) based on review of all available information, there is no evidence to suggest that the reported event is related to any design or manufacturing issues.The cause of the infection and subsequent revision cannot be conclusively determined; however, it is most likely related to the patient¿s underlying condition.

• Brand Name: EQUINOXE
• Common Device Name: RS GLENOID PLATE L POST AUG, 8 DEG, LEFT
• Manufacturer (Section D): EXACTECH, INC.; 2320 nw 66 court; gainesville FL 32653
• Manufacturer (Section G): EXACTECH, INC.; 2320 nw 66 ct; gainesville FL 32653
• Manufacturer Contact: kate jacobson ; 3523771140
• MDR Report Key: 12165679
• Report Number: 1038671-2021-00338
• Device Sequence Number: 17108006
• Product Code: KWT
• UDI-Device Identifier: 10885862186683
• UDI-Public: 10885862186683
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K110708
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2021
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 11/23/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 320-15-03
• Device Catalogue Number: 320-15-03
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 06/24/2021
• Supplement Date Received by Manufacturer: 11/03/2021
• Initial Report FDA Received Date: 07/14/2021
• Supplement Report FDA Received Date: 11/23/2021
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 06/12/2017
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: SEE H10
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 70 YR
• Patient Sex: Male